Shape-stabilization of organic phase change materials as mechanically stable silica boards with high latent heats synthesized via sol-gel route

被引:8
|
作者
Marske, Felix [1 ,2 ]
Haupt, Caroline [3 ,4 ]
Birkemeyer, Claudia [5 ]
Bacia, Kirsten [3 ,4 ]
Hahn, Thomas [1 ]
Enke, Dirk [6 ]
机构
[1] Martin Luther Univ Halle Wittenberg, Inst Tech Chem, D-06120 Halle, Germany
[2] Tech Univ Berlin, Inst Chem, D-10623 Berlin, Germany
[3] Martin Luther Univ Halle Wittenberg, Inst Chem, Biophys Chem, D-06120 Halle, Germany
[4] Martin Luther Univ Halle Wittenberg, Charles Tanford Prot Ctr, D-06120 Halle, Germany
[5] Univ Leipzig, Inst Analyt Chem, D-04103 Leipzig, Germany
[6] Univ Leipzig, Inst Chem Technol, D-04109 Leipzig, Germany
来源
关键词
Thermal energy storage; Phase change materials; Encapsulation; Sol-gel; Paraffin; Shape-stability; THERMAL-ENERGY STORAGE; CONDUCTIVITY ENHANCEMENT; PERFORMANCE EVALUATION; POROUS SCAFFOLDS; COMPOSITE; PCM; NITRIDE; NANOPARTICLES; SURFACTANTS; STABILITY;
D O I
10.1016/j.jobe.2022.105198
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
Monolithic shape-stabilized phase change materials (ss-PCM) are of great interest for energy -saving construction materials, solar-water heating systems and passive cooling systems of bat-teries and photovoltaic cells. However, the application range of ss-PCMs is currently limited by either low mechanical stabilities or low heat storage capacities. Therefore, we recently developed ss-PCMs based on silica and butyl stearate (BS) with high compressive strengths (1.2 MPa, 10 degrees C), but only moderate latent heats (-100 J/g). Here, we focus on validating the applicability of our porogen-assisted sol-gel process to other organic PCMs apart from butyl stearate. To increase the latent heat of ss-PCMs, we create a mixture of 70% hexadecane (HD) or octadecane (OD) with 30% BS and combine this PCM mixture with our novel-sol-gel route to synthesize ss-PCMs with high compressive strengths (1.2 MPa, 5 degrees C) as well as high latent heats (160 J/g). Due to the well -interconnected silica matrix confining the paraffins, the ss-PCMs have 70% higher thermal con-ductivities (0.43 W/mK, 5 degrees C) than pure paraffins, high shape-stabilities (-100%), high PCM loadings (83 wt%), and high chemical and long-term stabilities (>3000 thermal cycles). More-over, they are thermally stable up to-170 degrees C with PCM melting points of 17 degrees C and 22 degrees C. We also synthesize ss-PCMs with pure polyethylene glycol 600 (PEG600) and pure acetamide (Ac) to analyze the effect of non-paraffinic PCMs on the physicochemical properties of ss-PCMs. These ss-PCMs have a-30% lower latent heat than expected because the PCM either reacts strongly by hydrogen bonding with the silica (PEG600) or was chemically degraded under the basic condi-tions during gelation (Ac). In contrast to the low compressive strength of shape-stabilized PEG600 (35 kPa, 5 degrees C), the ss-PCMs based on Ac have high compressive strengths (9.6 MPa, 5 degrees C). Moreover, they are translucent above the PCM melting point due to a nanoscopic silica matrix. The high supercooling effect (37 degrees C) and the moderate long-term stability (3000 thermal cycles, 20% lower latent heat) of shape-stabilized Ac restrict its application to special, glassy materials.
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页数:19
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